Progressive myoclonic epilepsy type 1

Disease Export to PDF
Name:
Progressive myoclonic epilepsy type 1
Description:
A rare progressive myoclonic epilepsy (PME) disorder characterized by action- and stimulus-sensitive myoclonus, and tonic-clonic seizures with ataxia, but with only a mild cognitive decline over time.
ORPHAcode:
308
Synonyms:
EPM1
Progressive myoclonus epilepsy type 1
ULD
Unverricht-Lundborg disease
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14